Partial hypoxanthine-guanine phosphoribosyltransferase deficiency presenting as acute renal failure (Q46766516)

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scientific article published on 21 October 2005

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Language	Label	Description	Also known as
English	Partial hypoxanthine-guanine phosphoribosyltransferase deficiency presenting as acute renal failure	scientific article published on 21 October 2005

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16240158

retrieved

25 December 2017

reference URL

http://europepmc.org/abstract/MED/16240158

title

Partial hypoxanthine-guanine phosphoribosyltransferase deficiency presenting as acute renal failure (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16240158

retrieved

25 December 2017

reference URL

http://europepmc.org/abstract/MED/16240158

author name string

Sarah Cherian

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16240158

retrieved

25 December 2017

reference URL

http://europepmc.org/abstract/MED/16240158

Charles H Crompton

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16240158

retrieved

25 December 2017

reference URL

http://europepmc.org/abstract/MED/16240158

publication date

21 October 2005

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16240158

retrieved

25 December 2017

reference URL

http://europepmc.org/abstract/MED/16240158

published in

Pediatric Nephrology

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16240158

retrieved

25 December 2017

reference URL

http://europepmc.org/abstract/MED/16240158

volume

20

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16240158

retrieved

25 December 2017

reference URL

http://europepmc.org/abstract/MED/16240158

issue

12

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16240158

retrieved

25 December 2017

reference URL

http://europepmc.org/abstract/MED/16240158

page(s)

1811-1813

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16240158

retrieved

25 December 2017

reference URL

http://europepmc.org/abstract/MED/16240158

cites work

Partial hypoxanthine-Guanine phosphoribosyltransferase deficiency as the unsuspected cause of renal disease spanning three generations: a cautionary tale

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16240158

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Purine enzyme defects as a cause of acute renal failure in childhood

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16240158

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal serum uric acid levels in children

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16240158

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The pathogenesis of the Lesch-Nyhan syndrome: ATP use is positively related to hypoxanthine supply to hypoxanthine guanine phosphoribosyltransferase

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16240158

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Purine metabolism in Lesch-Nyhan syndrome versus Kelley-Seegmiller syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16240158

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inherited defects of purine and pyrimidine metabolism: Laboratory methods for diagnosis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16240158

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical correlations in partial hypoxanthine guanine phosphoribosyltransferase deficiency

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16240158

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A role for uric acid in the progression of renal disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16240158

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

New mutations of the HPRT gene in Lesch-Nyhan syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16240158

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Childhood hyperuricemia and acute renal failure resulting from a missense mutation in the HPRT gene

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16240158

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S00467-005-2065-8

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16240158

retrieved

25 December 2017

reference URL

http://europepmc.org/abstract/MED/16240158

PubMed publication ID

16240158

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16240158

retrieved

25 December 2017

reference URL

http://europepmc.org/abstract/MED/16240158

 

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